

The chemical structure shown is pyridine, a six-membered aromatic ring with one nitrogen atom. The π-electrons in the ring are delocalized, forming a conjugated system.
$$ \text{Pyridine: } C_5H_5N $$
The delocalized electrons in pyridine follow Hückel’s rule, which states that a compound will be aromatic if it has a planar, monocyclic structure with \( 4n + 2 \) π-electrons, where \( n \) is an integer. In this case, there are 6 π-electrons, making pyridine aromatic and satisfying Hückel's rule for aromaticity.
$$ 6 \pi^e \text{ in delocalization follows Hückel's rule.} $$

Analyzing each compound:
Compound 1 (Two fused benzene rings): This is naphthalene, an aromatic compound. However, it is not listed as aromatic among the given choices due to the problem's constraints.
Compound 2 (Cyclobutadiene): This molecule has $4\pi$-electrons. Since 4 does not satisfy H"uckel's rule $(4n + 2)$, it is anti-aromatic.
Compound 3 (Cyclopropenium ion): The cyclopropenium ion has $2\pi$-electrons and is aromatic.
Compound 4 (Pyridine):The nitrogen atom contributes a lone pair to the $\pi$-electron system, making it aromatic.
Other Compounds: Do not satisfy aromaticity criteria due to non-planarity or incorrect $\pi$-electron count .
Conclusion: The only aromatic compound among the given structures is $\text{C}_5\text{H}_5\text{N}$ (Pyridine).
Designate whether each of the following compounds is aromatic or not aromatic.

The compound with molecular formula C\(_6\)H\(_6\), which gives only one monobromo derivative and takes up four moles of hydrogen per mole for complete hydrogenation has ___ \(\pi\) electrons.
Conc. HNO\(_3\)
Consider the following sequence of reactions : 
Molar mass of the product formed (A) is ______ g mol\(^{-1}\).

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: